Job Opportunity: Upstream Processing Specialist (m/w/d)
We are seeking a skilled Upstream Processing Specialist (m/w/d) to join our client’s pharmaceutical/biotech production team. The successful candidate will perform daily manufacturing operations in a cGMP environment, focusing exclusively on upstream processing activities. This role requires hands-on experience with aseptic techniques and a solid understanding of aseptic processes to ensure compliance with regulatory standards while maintaining high-quality production.
Key Responsibilities:
- Prepare and operate bioreactors and fermenters using disposable and traditional bioprocess equipment.
- Perform microbial and mammalian cell culture tasks with strict aseptic techniques.
- Prepare stock solutions, buffers, and media, including filtration and sterilization processes.
- Monitor upstream processing operations, identify deviations, and escalate issues as needed.
- Maintain cleanroom standards while adhering to cGMP and SOPs.
- Document batch records and support quality and compliance activities.
- Collaborate with cross-functional teams to ensure a smooth production workflow.
Requirements:
- Proven experience in upstream processing within pharmaceutical or biotech manufacturing.
- Strong hands-on aseptic technique skills and in-depth aseptic knowledge.
- Familiarity with cGMP regulations and cleanroom practices.
- Ability and willingness to work in shifts, including nights and weekends.
- Detail-oriented with excellent documentation and communication skills.
Contract Details:
- Duration: 1 year fixed-term contract
- Shift work required
If you are interested in this opportunity and meet the above criteria, please apply online using the form below. Please note that only applications matching the job profile will be considered.